gastric or intestine surgery
Conditions
Interventions
Total:epidural saline control group (Group C, L2-L3 puncture, saline), intravenous lidocaine group (Group IV, L2-L3 puncture, saline epidural, intravenous lidocaine 1mg/kg), epidural lidocaine group I
Sponsors
Department of Anesthesiology, the First Affiliated Hospital, School of Medicine, Zhejiang University
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Aged 25 -65 yr,weighing 45-85 kg, with ASA physical status I -II, undergoing gastric or intestine surgery were enrolled in this study.
Exclusion criteria
Exclusion criteria: Any history of cardiovascular, psychological or neurological diseases, alcohol abuse, long-term use of sedative drugs, opioids and liver enzyme induction or inhibition medicine.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The induction (BIS reach 60) doses of propofol;plasma concentration of propofol; | — |
Secondary
| Measure | Time frame |
|---|---|
| target effect site concentration of propofol(BIS reach 60);The BIS-values at different time points;plasma concentration of lidocaine;the induction time (BIS reach 60);The sensory block level after the epidural injection; | — |
Countries
China
Contacts
Public ContactYan Xiang
Outcome results
None listed